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Millennium

Avalign Technologies, Inc. · Model 72-9850 · UDI-DI 00190776205447

KYT Prescription
6
510(k) clearances
10
Adverse events
1
Recalls
159
Facilities

Description

LED Headlight System w Headband and Battery

Recalls

DateFirmReason
2023-03-20DermLite LLCIncorrect labeling; Package labeling contains a different serial number then the serial number on the product labeling.

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.